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Completed

NCT Number: NCT04097834

Integrating PrEP Into Family Planning Services at Title X Clinics in the Southeastern US

Pre-exposure Prophylaxis (PrEP) is a daily pill to prevent HIV that, when taken as prescribed, reduces the risk of getting HIV from sexual intercourse or drug use. In the United States, most studies which examine prescribing PrEP have not included young women. PrEP provides a way for women to take control of their HIV prevention and may be a good option for some women.

Family planning clinics are a trusted source of preventative, routine, and symptom-driven gynecological care for adolescent and young adult women (AYAW). Thus, these clinics are a natural setting to provide PrEP services for AYAW. This study will examine how effectively three clinics in Atlanta are able to implement a PrEP program for their eligible female patients as well as follow a cohort of 300 women for six months (150 starting PrEP immediately and 150 electing to not take PrEP, at least initially) to characterize individual, provider, and clinic-level variables and constructs that are associated with PrEP uptake, continuation, and adherence.

Both participant and biological data will be collected to answer the primary research question. Women will provide blood, urine, oral, vaginal, anal, and hair samples at three different time points. These samples will be tested to measure incident sexually transmitted infections and unplanned pregnancies as well as PrEP adherence (for women who initiated PrEP). Ultimately, this data will describe each clinic's effectiveness at providing PrEP services to AYAW.

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Key information

Conditions

HIV Infections Blood-Borne Infections Communicable Diseases Genital Diseases Immune System Diseases Immunologic Deficiency Syndromes Infections Lentivirus Infections RNA Virus Infections Retroviridae Infections Sexually Transmitted Diseases Sexually Transmitted Diseases, Viral Urogenital Diseases Virus Diseases

Age range

13 year–45 year

Sex eligibility

Female

Study type

Observational

Primary location

Emory University

Atlanta, Georgia, 30322, United States

About this study

Planning4PrEP is a mixed hybrid Type 1 effectiveness implementation study of three family planning clinics in Atlanta integrating PrEP into their services and evaluating the multi-level factors associated with PrEP reach, level of adoption, and implementation (e.g., PrEP screening and prescription) within and across these clinics while also evaluating the effect on PrEP uptake, continuation, and adherence over a six-month follow-up period. Variation exists among types of family planning clinics, and this variation could have an impact on how clinics decide to implement, integrate, and even sustain PrEP services. This study will evaluate three family planning clinics as they adopt and sustain PrEP into their routine services to capture details of the implementation process unique to each clinic type, as well as commonalities across the clinics, with the ultimate aim to evaluate the impact of the implementation on the primary outcome (PrEP uptake, adherence, and continuation).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be self-identified as born female
  • Must be able to be provide written informed consent
  • Must be able to speak and understand English as determined by staff during recruitment
  • Must be 13-45 years old at time of consent
  • Must have been seen for a patient visit in one of the three implementation clinics during the preceding 60 days and identified as a PrEP candidate based on point-of-care HIV testing and risk assessment

Exclusion criteria

  • HIV-infected at the time of screening by self-report or screening laboratory assessment
  • Currently enrolled in an HIV vaccine trial
  • Has any condition that in the opinion of study staff would make participation in the study unsafe or interfere with achieving study objectives
  • Has been on PrEP for 7 or more consecutive days in the past
  • Currently receiving PrEP services at any location outside the 3 implementation clinics
  • Currently participating in another PrEP or candidate PrEP study

Treatment and study plan

Primary outcomes

  1. Proportion of participants with a PrEP prescription at baseline who initiate PrEP

    Time frame: 6 months post enrollment

    Among participants with a PrEP prescription at baseline, the proportion who initiate PrEP measured via pharmacy prescription fill data, medical chart abstraction, and participant self-report

  2. Proportion of participants with a PrEP prescription at baseline who attend at least one follow-up visit and have at least one documented PrEP prescription refill during each 3-month interval

    Time frame: 6 months post enrollment

    Among participants with a PrEP prescription at baseline, the proportion who continue their PrEP regimen evidenced by pharmacy prescription fill data, medical chart abstraction, and participant self-report

  3. Percentage of participants with a PrEP prescription at baseline who adhere to their PrEP regimen

    Time frame: 6 months post enrollment

    Among participants with a PrEP prescription at baseline, percentage who adhere to PrEP, defined by 3 data sources at each follow-up visit-pharmacologic, self-report, and pharmacy. Pharmacological data will include: average ng/mg tenofovir (TFV) concentration measured via hair sample; percentage of participants with adherence level consistent with 7 doses/week (TFV ng/mL≥ 0.0370 ng/mL); percentage of participants with dried blood spot TFV concentration≥1250 fmol/punch; percentage of participants with urine TFV immunoassay detected. Self-report data will include: percentage of participants reporting no missed doses in the past 7 days; percentage of participants reporting very good or excellent adherence (5 or 6 on a 6-level scale) in the past 30 days; percentage of participants who self-report adherence of ≥90%. Pharmacy fill data will include: percentage of participants with 80% adherence measured by medication possession ratio (the # of dispensed pills/# of days since starting PrEP)

Secondary outcomes

  1. Incidence rate of Neisseria gonorrhea among each participant group

    Time frame: 3- and 6-months post enrollment

    For each participant group (those with and those without a PrEP prescription at baseline) the incidence rate of STIs per total follow-up period will be calculated as the ratio of new STI infections (confirmed via multiplex PCR testing or chart review) to the total amount of person-time in each group

  2. Incidence rate of Chlamydia trachomatis among each participant group

    Time frame: 3- and 6-months post enrollment

    For each participant group (those with and those without a PrEP prescription at baseline) the incidence rate of STIs per total follow-up period will be calculated as the ratio of new STI infections (confirmed via multiplex PCR testing or chart review) to the total amount of person-time in each group

  3. Incidence rate of Trichomonas vaginalis among each participant group

    Time frame: 3- and 6-months post enrollment

    For each participant group (those with and those without a PrEP prescription at baseline) the incidence rate of STIs per total follow-up period will be calculated as the ratio of new STI infections (confirmed via multiplex PCR testing or chart review) to the total amount of person-time in each group

  4. Incidence rate of unintended pregnancy among each participant group

    Time frame: 3- and 6-months post enrollment

    For each participant group (those with and those without a PrEP prescription at baseline) the incidence rate of unintended pregnancies (pregnancies that do not match a participant's self-reported pregnancy intentions) per total follow-up period will be calculated as the ratio of new pregnancies (confirmed via positive urine pregnancy test) to the total amount of person-time in each group

  5. Incidence rate of HIV infection among each participant group

    Time frame: 3- and 6-months post enrollment

    For each participant group (those with and those without a PrEP prescription at baseline) the incidence rate of HIV infection per total follow-up period will be calculated as the ratio of new HIV infections (defined as a positive HIV test based on an FDA-approved HIV test with confirmatory negative testing of samples collected at baseline) to the total amount of person-time in each group

  6. Proportion of participants among each participant group reporting contraception use

    Time frame: Enrollment and 3- and 6-months post enrollment

    For each participant group (those with and those without a PrEP prescription at baseline), contraception use will be calculated as the percentage of participants who self-report use of a CDC-defined Tier 1 or Tier 2 contraception method

  7. Proportion of participants among each participant group reporting current contraception type

    Time frame: Enrollment and 3- and 6-months post enrollment

    For each participant group (those with and those without a PrEP prescription at baseline), contraception type will be determined as the self-reported current contraception type used

  8. Proportion of participants adherent to current contraceptive method measured among each participant group

    Time frame: Enrollment and 3- and 6-months post enrollment

    Proportion of participants adherent to current contraceptive method measured among each participant group via self-report

  9. Proportion of participants who are clinically-indicated to initiate PrEP

    Time frame: 3- and 6-months post enrollment

    Among all participants, the proportion of participants whose current clinical and behavioral profile indicate, per CDC clinical practice guidelines, they could begin PrEP, measured via STI testing, medical chart review, and self-report

  10. Proportion of participants who indicate interest in initiating PrEP

    Time frame: Enrollment and 3- and 6-months post enrollment

    Among all participants, the proportion of participants who report interest in beginning PrEP via interviewer-administered questionnaire and self-report

  11. Proportion of all participants who initiate PrEP

    Time frame: Enrollment and 3- and 6-months post enrollment

    Among all participants, the proportion of participants with a PrEP-prescription, pharmacy-confirmed fill of their PrEP prescription, and who self-report initiating PrEP

Sponsors and collaborators

Lead sponsor

University of North Carolina, Chapel Hill

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • National Institute of Mental Health (NIMH)
  • National Institute on Drug Abuse (NIDA)

Registry information

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Sep 20, 2019
Registry last updated
May 10, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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